Primary Device ID | 00810125991080 |
NIH Device Record Key | d0b28742-8c7f-4ceb-81fd-fb8e001967ce |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ET RIGID RETRACTION CAP |
Version Model Number | ETRRC440C |
Company DUNS | 796083090 |
Company Name | HIOSSEN, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00810125991080 [Primary] |
NDP | Accessories, Implant, Dental, Endosseous |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-07-05 |
Device Publish Date | 2024-06-27 |
00810019240348 | ETRRC760 |
00810019240331 | ETRRC670 |
00810019240324 | ETRRC660 |
00810019240317 | ETRRC640 |
00810019240300 | ETRRC570 |
00810019240294 | ETRRC560 |
00810019240287 | ETRRC540 |
00810019240270 | ETRRC471 |
00810019240263 | ETRRC461 |
00810019240256 | ETRRC441 |
00810019240249 | ETRRC470 |
00810019240232 | ETRRC460 |
00810019240225 | ETRRC440 |
00810125991097 | ETRRC460C |
00810125991080 | ETRRC440C |
00810125991202 | ETRRC760C |
00810125991196 | ETRRC670C |
00810125991189 | ETRRC660C |
00810125991172 | ETRRC640C |
00810125991165 | ETRRC570C |
00810125991158 | ETRRC560C |
00810125991141 | ETRRC540C |
00810125991134 | ETRRC471C |
00810125991127 | ETRRC461C |
00810125991110 | ETRRC441C |
00810125991103 | ETRRC470C |